UDI device identifier
Revolution Rotational Imaging Catheter 89000
UDI device identifier 00184360000358 · Philips Image Guided Therapy Corporation
Key facts
| Primary DI | 00184360000358 |
|---|---|
| Brand name | Revolution Rotational Imaging Catheter |
| Version or model | 89000 |
| Catalog number | 89000 |
| Company | Philips Image Guided Therapy Corporation |
| DUNS number | 018860556 |
| Product code | OBJ |
| GMDN term | Intravascular ultrasound imaging catheter, single-use |
| Premarket submission | K050995 |
| Device class | Class II |
| Single use | Yes |
| Packaged sterile | Yes |
| Implantable | No |
| Publish date | Aug 23, 2016 |
| Version date | Aug 20, 2024 |
At a glance
- 10–99 MAUDE reports citing this UDI
- Yes Linked premarket submission
- Yes EUDAMED counterpart found
- 100–999 GUDID devices with this product code
Counts are shown as ranges. Exact figures, trends and every underlying record are available in Orca1.
About UDI device identifiers (GUDID)
The Global Unique Device Identification Database (GUDID) holds the device identifiers (UDI-DIs) and key attributes that labelers submit to the FDA for devices that carry a unique device identifier.
Source: U.S. FDA Global Unique Device Identification Database (GUDID), via NLM AccessGUDID · Source date: